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  2. Sodium cyanide - Wikipedia

    en.wikipedia.org/wiki/Sodium_cyanide

    Sodium cyanide is a compound with the formula Na C N and the structure Na + − C≡N. It is a white, water-soluble solid. Cyanide has a high affinity for metals, which leads to the high toxicity of this salt. Its main application, in gold mining, also exploits its high reactivity toward metals. It is a moderately strong base.

  3. List of UN numbers 1601 to 1700 - Wikipedia

    en.wikipedia.org/wiki/List_of_UN_numbers_1601_to...

    n.o.s. = not otherwise specified meaning a collective entry to which substances, mixtures, solutions or articles may be assigned if a) they are not mentioned by name in 3.2 Dangerous Goods List AND b) they exhibit chemical, physical and/or dangerous properties corresponding to the Class, classification code, packing group and the name and description of the n.o.s. entry [2]

  4. Cyanide - Wikipedia

    en.wikipedia.org/wiki/Cyanide

    Among the most toxic cyanides are hydrogen cyanide (HCN), sodium cyanide (NaCN), potassium cyanide (KCN), and calcium cyanide (Ca(CN) 2). The cyanide anion is an inhibitor of the enzyme cytochrome c oxidase (also known as aa 3), the fourth complex of the electron transport chain found in the inner membrane of the mitochondria of eukaryotic ...

  5. Cyanate - Wikipedia

    en.wikipedia.org/wiki/Cyanate

    Sodium cyanate is isostructural with sodium fulminate, confirming the linear structure of the cyanate ion. [3] It is made industrially by heating a mixture of sodium carbonate and urea. [4] Na 2 CO 3 + 2 OC(NH 2) 2 → 2 NaNCO + CO 2 + 2 NH 3 + H 2 O. A similar reaction is used to make potassium cyanate. Cyanates are produced when cyanides are ...

  6. Acyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Acyl_cyanide

    In organic chemistry, an acyl cyanide is a functional group with the formula R−C(O)CN and structure R−C(=O)−C≡N. It consists of an acyl group (R−C=O) attached to cyanide (−C≡N). Examples include acetyl cyanide, formyl cyanide, and oxalyl dicyanide. Acyl cyanides are reagents in organic synthesis. [1] [2]

  7. Cyanogen - Wikipedia

    en.wikipedia.org/wiki/Cyanogen

    Cyanogen is typically generated from cyanide compounds. One laboratory method entails thermal decomposition of mercuric cyanide: . 2 Hg(CN) 2 → (CN) 2 + Hg 2 (CN) 2 Or, one can combine solutions of copper(II) salts (such as copper(II) sulfate) with cyanides; an unstable copper(II) cyanide is formed which rapidly decomposes into copper(I) cyanide and cyanogen.

  8. Cyanogen azide - Wikipedia

    en.wikipedia.org/wiki/Cyanogen_azide

    Cyanogen azide is a chemical compound with the chemical formula C N 4, or more precisely − N=N + =N−C≡N.It is an azide compound of carbon and nitrogen.It is an oily, colourless liquid at room temperature. [2]

  9. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    Reaction of the sodium cyanoacetate with ethyl bromide in an aqueous–organic two-phase system in the presence of a phase transfer catalyst. [ 4 ] Oxidation of 3-ethoxypropionitrile, an ether , with oxygen under pressure in the presence of cobalt(II) acetate tetrahydrate as catalyst and N -hydroxyphthalimide as a radical generator.